Manufacturer of medical devices registered in the European database in Tuttlingen, Germany.
| Registration number (SRN) | DE-MF-000005504 |
|---|---|
| Role | Manufacturer |
| Status | Active |
| Country | Germany |
| City | 78532 Tuttlingen |
| Address | Am Aesculap-Platz, 78532 Tuttlingen |
| Registered on | 2021-05-27 |
| FDA establishment register | Registered with the U.S. FDA |
|---|---|
| Matched entry | AESCULAP AG (DE) · FDA 9610612 |
| Certificate | Status | Expiry | Type | Body |
|---|---|---|---|---|
G12 010066 0441 | supplemented | expired 2026-06-30 | Quality management system | NB 0123 |
G11 010066 0437 | reissued | 2030-07-09 | Quality management system | NB 0123 |
G10 010066 0438 | reissued | 2030-07-09 | Quality management system | NB 0123 |
20003GB450260622 | reissued | 2031-06-22 | Technical documentation | NB 0482 |
⚠️ State of the register on 2026-08-20. EUDAMED shows only the current version of a certificate — earlier versions are not published, by the Commission or by anyone. A certificate shown as valid here may have changed since. For a legally binding check, consult EUDAMED directly.
The SRN is the registration number assigned by the European Commission. It has been mandatory since 28 May 2026 for any operator placing a medical device on the Union market. Contact details are published in the official register; we do not reproduce them here.
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